Canonical Allele Identifier: CA2670197273
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25156856dup , CM000666.2:g.25156856dup GRCh38
NC_000004.11:g.25158478dup , CM000666.1:g.25158478dup GRCh37
NC_000004.10:g.24767576dup NCBI36
NG_028222.1:g.8728dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.388+1dup
ENST00000680581.1:c.388+1dup
ENST00000680824.1:n.1604+1dup
ENST00000681071.1:n.680+1dup
ENST00000681166.1:n.1435+1dup
ENST00000681341.1:n.1529+1dup
ENST00000681640.1:n.482+1dup
ENST00000681948.1:c.643+1dup
ENST00000358971.7:c.*186+1dup
ENST00000382103.6:c.388+1dup
ENST00000514585.5:c.*89+1dup
NM_016955.3:c.388+1dup
XM_005248168.2:c.151+1dup
XM_006713965.2:c.208+1dup
XM_011513846.1:c.385+1dup
XM_011513847.1:c.355+1dup
XM_011513848.1:c.208+1dup
XM_011513846.2:c.385+1dup
XM_011513847.2:c.355+1dup
XM_017008277.1:c.643+1dup
XM_017008278.1:c.-36+1dup
NM_016955.4:c.388+1dup